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热休克蛋白70-伴侣蛋白3模块通过转录因子脂多糖诱导肿瘤坏死因子-α因子和集落刺激因子1调节巨噬细胞运动性和肿瘤浸润。

Hsp70-Bag3 Module Regulates Macrophage Motility and Tumor Infiltration via Transcription Factor LITAF and CSF1.

作者信息

Avinery Lena, Gahramanov Valid, Hesin Arkadi, Sherman Michael Y

机构信息

Department of Molecular Biology, Ariel University, Ariel 407000, Israel.

出版信息

Cancers (Basel). 2022 Aug 28;14(17):4168. doi: 10.3390/cancers14174168.

Abstract

The molecular chaperone Hsp70 has been implicated in multiple stages of cancer development. In these processes, a co-chaperone Bag3 links Hsp70 with signaling pathways that control cancer development. Recently, we showed that besides affecting cancer cells, Hsp70 can also regulate the motility of macrophages and their tumor infiltration. However, the mechanisms of these effects have not been explored. Here, we demonstrated that the Hsp70-bound co-chaperone Bag3 associates with a transcription factor LITAF that can regulate the expression of inflammatory cytokines and chemokines in macrophages. Via this interaction, the Hsp70-Bag3 complex regulates expression levels of LITAF by controlling its proteasome-dependent and chaperone-mediated autophagy-dependent degradation. In turn, LITAF regulates the expression of the major chemokine CSF1, and adding this chemokine to the culture medium reversed the effects of Bag3 or LITAF silencing on the macrophage motility. Together, these findings uncover the Hsp70-Bag3-LITAF-CSF1 pathway that controls macrophage motility and tumor infiltration.

摘要

分子伴侣Hsp70与癌症发展的多个阶段有关。在这些过程中,共伴侣Bag3将Hsp70与控制癌症发展的信号通路联系起来。最近,我们发现除了影响癌细胞外,Hsp70还可以调节巨噬细胞的运动及其肿瘤浸润。然而,这些作用的机制尚未得到探索。在这里,我们证明与Hsp70结合的共伴侣Bag3与转录因子LITAF相关联,LITAF可以调节巨噬细胞中炎性细胞因子和趋化因子的表达。通过这种相互作用,Hsp70-Bag3复合物通过控制其蛋白酶体依赖性和伴侣介导的自噬依赖性降解来调节LITAF的表达水平。反过来,LITAF调节主要趋化因子CSF1的表达,并且将这种趋化因子添加到培养基中可逆转Bag3或LITAF沉默对巨噬细胞运动的影响。总之,这些发现揭示了控制巨噬细胞运动和肿瘤浸润的Hsp70-Bag3-LITAF-CSF1途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f901/9454964/6a250b49bc6b/cancers-14-04168-g001.jpg

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